105516-73-2Relevant academic research and scientific papers
Me3Al-mediated domino nucleophilic addition/intramolecular cyclisation of 2-(2-oxo-2-phenylethyl)benzonitriles with amines; a convenient approach for the synthesis of substituted 1-aminoisoquinolines
Adusumalli, Krishna M. S.,Battula, Venkateswara R.,Gandham, Hima B.,Konidena, Lakshmi N. S.,Kumari, Krishnaiah,Namballa, Hari K.,Nidasanametla, Satya K. R.,Valluru, Krishna R.
, p. 2765 - 2772 (2022/01/12)
A simple and efficient protocol for the construction of 1-aminoisoquinolines was achieved by treating 2-(2-oxo-2- phenylethyl)benzonitriles with amines in the presence of Me3Al. The reaction proceeds via a domino nucleophilic addition with subsequent intr
Thermal or Lewis acid-promoted electrocyclisation and hetero Diels-Alder cycloaddition of α,β-unsaturated (conjugated) carbodiimides: A facile synthesis of nitrogen-containing heterocycles
Saito, Takao,Ohkubo, Takahiro,Kuboki, Hideki,Maeda, Masayuki,Tsuda, Kensaku,Karakasa, Takayuki,Satsumabayashi, Sadayoshi
, p. 3065 - 3080 (2007/10/03)
α,β-Diarylvinyl- and α-styryl-carbodiimides, prepared by the aza-Wittig reaction of iminophosphoranes with isocyanates, underwent either 6π-electrocyclisation upon heating or a Diels-Alder reaction under thermal or Lewis acid-promoted conditions with appr
CONJUGATED HETEROCUMULENES. SYNTHESIS OF C=C-CONJUGATED CARBODIIMIDES BY A WITTIG-TYPE REACTION OF IMINOPHOSPHORANES WITH ISOCYANATES AND THEIR CYCLOADDITIONS
Saito, Takao,Nakane, Michio,Endo, Masanobu,Yamashita, Hiromi,Oyamada, Yoko,Motoki, Shinichi
, p. 135 - 138 (2007/10/02)
A Wittig-type reaction of N-(1,2-diarylethenyl)iminophosphoranes with isocyanates gave C=C-conjugated carbodiimides, which were utilized in the synthesis of heterocycles.
